方案
99%
表单
crystals
mp
125-128 °C (lit.)
SMILES字符串
OC(=O)\C(Cl)=C(/Cl)C=O
InChI
1S/C4H2Cl2O3/c5-2(1-7)3(6)4(8)9/h1H,(H,8,9)/b3-2+
InChI key
LUMLZKVIXLWTCI-NSCUHMNNSA-N
正在寻找类似产品? 访问 产品对比指南
警示用语：
Danger
危险声明
危险分类
Acute Tox. 3 Oral - Eye Dam. 1 - Skin Corr. 1B - STOT SE 3
靶器官
Respiratory system
储存分类代码
6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
WGK
WGK 2
闪点(°F)
366.8 °F
闪点(°C)
186 °C
个人防护装备
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges, type P3 (EN 143) respirator cartridges
法规信息
危险化学品
此项目有
L Kronberg et al.
Chemical research in toxicology, 5(6), 852-855 (1992-11-01)
Mucochloric acid, a genotoxic hydroxyfuranone found in chlorinated drinking water, was reacted with cytidine, adenosine, guanosine, and uridine. HPLC analyses with UV detection at 290 nm showed that one major product peak was formed in the reactions of cytidine, adenosine
Oxidation and radical intermediates associated with the glutathione conjugation of mucochloric acid.
R T LaLonde et al.
Chemical research in toxicology, 7(4), 482-486 (1994-07-01)
The inactivation of the drinking water mutagen mucochloric acid (MCA) by reduced glutathione (GSH) was linked to the formation of an MCA-GSH conjugate, a nonmutagen in the Salmonella typhimurium (TA100) plate incorporation assay. Anaerobic formation of MCA-GSH is found now
Ji Zhang et al.
Organic letters, 5(4), 553-556 (2003-02-14)
[reaction: see text] The first direct reductive amination of mucochloric acid (1) has been accomplished. Reaction of 1 with various alkyl, aryl, and benzylamines, followed by reduction in the same pot, provides an efficient method of obtaining N-benzyl-3,4-dichloro-1,5-dihydro-pyrrol-2-one and N-aryl
R T LaLonde et al.
Environmental and molecular mutagenesis, 22(3), 181-187 (1993-01-01)
A difference in biological response to enantiomers is not an uncommon observation and is, therefore, to be expected in various manifestations of genotoxicity. The bacterial mutagen mucochloric acid (2,3-dichloro-5-hydroxy-2(5H)-furanone) has one chiral center, at C-5, but this mutagen exists in
I R Politzer et al.
Archives of environmental contamination and toxicology, 20(3), 371-374 (1991-04-01)
Cyclodextrins form inclusion complexes with a wide range of guest molecules which wholly, or in part, fit into their hydrophobic cavity. Since no covalent bonds are formed in this complexation, the guests can subsequently be eluted. The possibility of such
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持